Canonical Allele Identifier: CA425415821

Gene: SNX17

Linked Data

• MyVariant Identifiers: chr2:g.27598002G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375135G>A , CM000664.2:g.27375135G>A	GRCh38
NC_000002.11:g.27598002G>A , CM000664.1:g.27598002G>A	GRCh37
NC_000002.10:g.27451506G>A	NCBI36
NG_009305.1:g.323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.756G>A MANE Select	ENSP00000233575.2:p.Glu252=
ENST00000233575.6:c.756G>A	ENSP00000233575.2:p.Glu252=
ENST00000427123.5:c.*566G>A	ENSP00000405399.1:n.*566G>A
ENST00000440760.5:c.*601G>A	ENSP00000399727.1:n.*601G>A
ENST00000453453.1:c.*283G>A	ENSP00000401922.1:n.*283G>A
ENST00000493711.1:n.473G>A
ENST00000494893.5:n.932G>A
ENST00000537606.5:c.681G>A	ENSP00000439208.1:p.Glu227=
NM_001267059.1:c.720G>A	NP_001253988.1:p.Glu240=
NM_001267060.1:c.681G>A	NP_001253989.1:p.Glu227=
NM_001267061.1:c.696G>A	NP_001253990.1:p.Glu232=
NM_014748.3:c.756G>A	NP_055563.1:p.Glu252=
NR_049782.1:n.1129G>A
NR_049783.1:n.1102G>A
NR_049784.1:n.1078G>A
NR_049785.1:n.1011G>A
NR_049786.1:n.960G>A
NR_049787.1:n.811G>A
NR_049788.1:n.741G>A
XM_011533203.1:c.114G>A	XP_011531505.1:p.Glu38=
XM_011533203.2:c.114G>A	XP_011531505.1:p.Glu38=
XM_017005405.2:c.114G>A	XP_016860894.1:p.Glu38=
NM_014748.4:c.756G>A MANE Select	NP_055563.1:p.Glu252=
NM_001267059.2:c.720G>A	NP_001253988.1:p.Glu240=
NM_001267061.2:c.696G>A	NP_001253990.1:p.Glu232=
NR_049782.2:n.1009G>A
NR_049783.2:n.982G>A
NR_049784.2:n.958G>A
NR_049785.2:n.891G>A
NR_049786.2:n.840G>A
NR_049787.2:n.691G>A
NR_049788.2:n.621G>A
NM_001267060.2:c.681G>A	NP_001253989.1:p.Glu227=